ClinGen Allele Registry
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Canonical Allele Identifier:
CA13590399
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.57668884C>T
GRCh37
chr12:g.58062667C>T
Linked Data - Sequence & Population
gnomAD v2:
12:58062667 C / T
gnomAD v3:
12:57668884 C / T
gnomAD v4:
chr12-57668884-C-T
Joint Max Group AF
0.65895673 (NFE)
Genomes Max Group AF
0.65895673 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10876993
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.57668884C>T , CM000674.2:g.57668884C>T
GRCh38
NC_000012.11:g.58062667C>T , CM000674.1:g.58062667C>T
GRCh37
NC_000012.10:g.56348934C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'